295 results on '"Barbouche, Mohamed-Ridha"'
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2. Increased IL-22 in cerebrospinal fluid of neuro-behçet’s disease patients
3. Regulatory T-cell dysfunction and cutaneous exposure to Staphylococcus aureus underlie eczema in DOCK8 deficiency
4. Development and comparative evaluation of SARS-CoV-2 S-RBD and N based ELISA tests in various African endemic settings
5. Incidence and risk factors of SARS-CoV-2 infection among workers in a public health laboratory in Tunisia
6. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry
7. A Novel Point-of-Care Rapid Diagnostic Test for Screening Individuals for Antibody Deficiencies
8. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity
9. A Longitudinal Study in Tunisia to Assess the Anti-RBD IgG and IgA Responses Induced by Three Different COVID-19 Vaccine Platforms
10. The Seven STAT3-Related Hyper-IgE Syndromes
11. Performance of GeneXpert ultra in the diagnosis of Tuberculous Cervical lymphadenitis in formalin fixed paraffin embedded tissues
12. Toward personalization of asthma treatment according to trigger factors
13. HBHA-IGRA and cytotoxic mediators release assays for the diagnosis of cervical tuberculous lymphadenitis
14. Contributors
15. Defects in intrinsic and innate immunity
16. Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families
17. Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels
18. New insights into physiopathology of immunodeficiency-associated vaccine-derived poliovirus infection; systematic review of over 5 decades of data
19. Specific immune responses in mice following subchronic exposure to acetamiprid
20. Genetics of Inborn Errors of Immunity in highly consanguineous Middle Eastern and North African populations
21. Correction to: The Seven STAT3‑Related Hyper‑IgE Syndromes
22. Comprehensive review of autoantibodies in patients with hyper-IgM syndrome
23. Diagnostic challenge in a series of eleven patients with hyper IgE syndromes
24. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity
25. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
26. African Society for Immunodeficiency (Asid) Guidelines for Diagnosis and Management of Inborn Errors of Immunity in Africa: Core Concept, Development and Initial Results
27. Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry
28. Increased T-bet/GATA-3 and ROR-γt /Foxp3 Ratios in Cerebrospinal Fluid as Potential Criteria for Definite Neuro-Behçet’s Disease
29. Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity
30. Consanguinity and Primary Immunodeficiencies
31. A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients
32. Glycoproteomic studies of IgE from a novel hyper IgE syndrome linked to PGM3 mutation
33. X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
34. Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients
35. Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012)
36. Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies
37. COVID-19 in Tunisia (North Africa): Seroprevalence of SARS-CoV-2 in the General Population of the Capital City Tunis
38. B Cells Specific CpG Induces High IL-10 and IL-6 Expression In Vitro in Neuro-Behçet’s Disease
39. CFP32 as a target to attenuate the heterogeneous antibody response against Mycobacterium tuberculosis antigens in different endemic settings
40. Diagnostic challenge in a series of eleven patients with hyper IgE syndromes.
41. COVID-19 in Tunisia (North Africa): IgG and IgG subclass antibody responses to SARS-CoV-2 according to disease severity
42. COVID-19 in Tunisia (North Africa): Seroprevalence of SARS-CoV-2 in the general population of the capital city Tunis
43. Editorial: Immune-Related Non-Communicable Diseases in Africa
44. Culture filtrate protein 32 as a potential target to attenuate the heterogeneous antibody response against Mycobacterium tuberculosis Antigens in different endemic settings
45. Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lymphoblastic leukemia
46. A Novel Point-of-Care Rapid Diagnostic Test for Screening Individuals for Antibody Deficiencies
47. Profound differences in IgE and IgG recognition of micro‐arrayed allergens in hyper‐IgE syndromes
48. A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients
49. Two distinct conformational states of Mycobacterium tuberculosis virulent factor early secreted antigenic target 6 kDa are behind the discrepancy around its biological functions
50. Clinical and Genetic Heterogeneity of Inherited Autosomal Recessive Susceptibility to Disseminated Mycobacterium bovis Bacille Calmette-Guérin Infection
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